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      Congress Must Update FDA Regulations for Medical AI

      Author(s): 1
      Publication date (Electronic):
      Journal: JAMA Health Forum
      Publisher: American Medical Association (AMA)

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          Abstract

          This JAMA Forum discusses pending legislation in the US House and Senate and the history of the “firm-based approach” the US Food and Drug Administration (FDA) could use when regulating artificial intelligence (AI) medical devices to augment patient care.

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          The future landscape of large language models in medicine

          Jan Clusmann, Fiona R. Kolbinger, Hannah Sophie Muti … (2023)
          Large language models (LLMs) are artificial intelligence (AI) tools specifically trained to process and generate text. LLMs attracted substantial public attention after OpenAI’s ChatGPT was made publicly available in November 2022. LLMs can often answer questions, summarize, paraphrase and translate text on a level that is nearly indistinguishable from human capabilities. The possibility to actively interact with models like ChatGPT makes LLMs attractive tools in various fields, including medicine. While these models have the potential to democratize medical knowledge and facilitate access to healthcare, they could equally distribute misinformation and exacerbate scientific misconduct due to a lack of accountability and transparency. In this article, we provide a systematic and comprehensive overview of the potentials and limitations of LLMs in clinical practice, medical research and medical education.
          Article 0 comments Cited 45 times – based on 0 reviews     Review now
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            The Role for Policy in AI-Assisted Medical Diagnosis

            David E. Newman-Toker, Joshua M. Sharfstein (2024)
            This JAMA Forum discusses the promise and pitfalls of using large language models and artificial intelligence (AI) in the diagnosis of patients.
            Article 0 comments Cited 1 times – based on 0 reviews     Review now
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              Strategies for Regulating Disruptive Medical Technologies

              Scott Gottlieb (2023)
              This JAMA Forum discusses 3 regulatory lessons from the US Food and Drug Administration that could be used for regulating new medical devices and technologies, such as those that include artificial intelligence.
              Article 0 comments Cited 1 times – based on 0 reviews     Review now
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                Author and article information

                Journal
                Title: JAMA Health Forum
                Abbreviated Title: JAMA Health Forum
                Publisher: American Medical Association (AMA)
                ISSN (Electronic): 2689-0186
                Publication date Created: July 05 2024
                Publication date (Electronic): July 11 2024
                Volume: 5
                Issue: 7
                Page: e242691
                Affiliations
                [1 ]American Enterprise Institute, Washington, DC
                Article
                DOI: 10.1001/jamahealthforum.2024.2691
                SO-VID: 414680c0-1e45-4121-85a2-cbb85bc96117
                Copyright © © 2024
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